Status:
COMPLETED
Determination of TOF Test Threshold for Obtaining Reliable Pedicle Screw Stimulation Test During Lumbar Spine Surgery
Lead Sponsor:
NYU Langone Health
Conditions:
Neuromuscular Blockade
Eligibility:
All Genders
18-85 years
Brief Summary
During lumbar spine fusion surgery intraoperative neurophysiological monitoring is in routine use for prevention of possible nerve injuries during placement of screw into pedicle. Pedicle screw stimul...
Eligibility Criteria
Inclusion
- Subjects undergoing lumbar spine fusion surgery with neurophysiologic intraoperative monitoring when pedicle screw stimulation test is performed.
- Subjects of both gender
- Age 18-85
- With diagnosis of lumbar spinal stenosis.
- All subjects capable of giving informed consent in order to be included for the study.
Exclusion
- Subjects with medical history of presence of neuromuscular disease
Key Trial Info
Start Date :
February 11 2015
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
January 8 2018
Estimated Enrollment :
46 Patients enrolled
Trial Details
Trial ID
NCT02285829
Start Date
February 11 2015
End Date
January 8 2018
Last Update
January 18 2018
Active Locations (1)
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1
NYU Langone Medical Center, Hospital for Joint Diseases
New York, New York, United States, 10003